U.S. flag

An official website of the United States government

nsv5513328

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 24 studies. See in: genome view    
Submitted genomic114,591,466-114,591,526Question Mark
Overlapping variant regions from other studies: 111 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):114,462,188-114,462,248Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5513328Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11114,591,466114,591,526
nsv5513328RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11114,462,188114,462,248

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052565deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052565Submitted genomicNC_000011.10:g.114
591466_114591526de
l
GRCh38 (hg38)NC_000011.10Chr11114,591,466114,591,526
nssv17052565RemappedPerfectNC_000011.9:g.1144
62188_114462248del
GRCh37.p13First PassNC_000011.9Chr11114,462,188114,462,248

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17052565<0.00126404
Support Center